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Highly enantioselective insertion of carbenoids into O-H bonds of phenols: an efficient approach to chiral alpha-aryloxycarboxylic esters.
J Am Chem Soc. 2007 Oct 24; 129(42):12616-7.JA

Authors+Show Affiliations

Chen C
State Key Laboratory and Institute of Elemento-organic Chemistry, Nankai University, Tianjin, China.
Zhu SF
No affiliation info available
Liu B
No affiliation info available
Wang LX
No affiliation info available
Zhou QL
No affiliation info available

MeSH

AlcoholsCarbonCatalysisChemistry, OrganicEstersHydrogenHydrogen BondingHydrolysisLigandsModels, ChemicalOxygenPhenolPhenolsStereoisomerism

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

17902665

Citation

Chen, Chao, et al. "Highly Enantioselective Insertion of Carbenoids Into O-H Bonds of Phenols: an Efficient Approach to Chiral Alpha-aryloxycarboxylic Esters." Journal of the American Chemical Society, vol. 129, no. 42, 2007, pp. 12616-7.
Chen C, Zhu SF, Liu B, et al. Highly enantioselective insertion of carbenoids into O-H bonds of phenols: an efficient approach to chiral alpha-aryloxycarboxylic esters. J Am Chem Soc. 2007;129(42):12616-7.
Chen, C., Zhu, S. F., Liu, B., Wang, L. X., & Zhou, Q. L. (2007). Highly enantioselective insertion of carbenoids into O-H bonds of phenols: an efficient approach to chiral alpha-aryloxycarboxylic esters. Journal of the American Chemical Society, 129(42), 12616-7.
Chen C, et al. Highly Enantioselective Insertion of Carbenoids Into O-H Bonds of Phenols: an Efficient Approach to Chiral Alpha-aryloxycarboxylic Esters. J Am Chem Soc. 2007 Oct 24;129(42):12616-7. PubMed PMID: 17902665.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Highly enantioselective insertion of carbenoids into O-H bonds of phenols: an efficient approach to chiral alpha-aryloxycarboxylic esters. AU - Chen,Chao, AU - Zhu,Shou-Fei, AU - Liu,Bin, AU - Wang,Li-Xin, AU - Zhou,Qi-Lin, Y1 - 2007/09/29/ PY - 2007/10/2/pubmed PY - 2008/1/17/medline PY - 2007/10/2/entrez SP - 12616 EP - 7 JF - Journal of the American Chemical Society JO - J Am Chem Soc VL - 129 IS - 42 SN - 0002-7863 UR - https://www.unboundmedicine.com/medline/citation/17902665/Highly_enantioselective_insertion_of_carbenoids_into_O_H_bonds_of_phenols:_an_efficient_approach_to_chiral_alpha_aryloxycarboxylic_esters_ L2 - https://doi.org/10.1021/ja074729k DB - PRIME DP - Unbound Medicine ER -